Canonical Allele Identifier: CA631619911
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs1187152354
gnomAD v2: 19-5903934-C-A
gnomAD v4: 19-5903923-C-A
MyVariant Identifiers: chr19:g.5903934C>A (hg19) chr19:g.5903923C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903923C>A , CM000681.2:g.5903923C>A GRCh38
NC_000019.9:g.5903934C>A , CM000681.1:g.5903934C>A GRCh37
NC_000019.8:g.5854934C>A NCBI36
NG_027808.1:g.5091G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.84G>T
NM_001193375.1:c.-215G>T NP_001180304.1:n.-215G>T
NM_175614.4:c.-215G>T NP_783313.1:n.-215G>T
NR_034166.2:n.91G>T
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